Sensitive

Inflammatory bowel disease

near ZBTB40 · rs12568930

Where this position leads

Condition: Inflammatory Bowel Disease

rs12568930 Condition: Inflammatory Bowel Disease Inflammatory Bowel Disease Condition rs12568930 rs12568930 near ZBTB40

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Inflammatory bowel disease — no copies of the reported risk allele. (GWAS Catalog, Nature 2012, PMID:23128233)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Inflammatory bowel disease. (GWAS Catalog, Nature 2012, PMID:23128233)
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Inflammatory bowel disease compared to the general population. (GWAS Catalog, Nature 2012, PMID:23128233)

Source: GWAS Catalog, Nature 2012, PMID:23128233

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs12568930

What is rs12568930?

rs12568930 is a single position in the genome, in or near the near ZBTB40 gene. Published research associates it with inflammatory bowel disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs12568930 linked to?

On MyGeneLog this position is linked to Inflammatory Bowel Disease. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs12568930?

Subjects that appear in the title or abstract of the same papers as this rsID include bones and fractures (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs12568930 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs12568930 come from?

GWAS Catalog, Nature 2012, PMID:23128233. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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